Official recall record
Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following: 35700BAX2 (Spectrum V8 infusion pu
- Issuing authority
- US FDA — Medical Devices
- Alert date
- 2024-07-17
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00085412498683
- Brand on record
- Baxter Healthcare Corporation
What the authority reported
The Spectrum WBM may fail to auto-document infusion status information back to the hospital's Electronic Medical Record (EMR) system. This software issue only impacts customers where the Spectrum V8 or Spectrum IQ infusion system is integrated with the hospital s EMR system.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 6 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2020-06-30 · US FDA — Medical Devices
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) - 2020-11-23 · US FDA — Medical Devices
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) - Product Usage: intended to be used for the co - 2024-11-19 · US FDA — Medical Devices
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2 - 2024-07-17 · US FDA — Medical Devices
Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 - 2025-11-28 · US FDA — Medical Devices
SIGMA Spectrum Infusion Pump, Model/Catalog Number: 35700BAX2
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